WO2005002334A1 - Formulations agrochimiques - Google Patents

Formulations agrochimiques Download PDF

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Publication number
WO2005002334A1
WO2005002334A1 PCT/EP2004/006673 EP2004006673W WO2005002334A1 WO 2005002334 A1 WO2005002334 A1 WO 2005002334A1 EP 2004006673 W EP2004006673 W EP 2004006673W WO 2005002334 A1 WO2005002334 A1 WO 2005002334A1
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WO
WIPO (PCT)
Prior art keywords
agrochemical active
optionally
formulations
agrochemical
formulation
Prior art date
Application number
PCT/EP2004/006673
Other languages
German (de)
English (en)
Inventor
Andreas Röchling
Frank Rosenfeldt
Original Assignee
Bayer Cropscience Aktiengesellschaft
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer Cropscience Aktiengesellschaft filed Critical Bayer Cropscience Aktiengesellschaft
Priority to NZ544450A priority Critical patent/NZ544450A/en
Priority to EP04740113A priority patent/EP1643833B1/fr
Priority to CA002530883A priority patent/CA2530883A1/fr
Priority to PL04740113T priority patent/PL1643833T3/pl
Priority to DE502004008588T priority patent/DE502004008588D1/de
Priority to US10/563,328 priority patent/US7655599B2/en
Priority to BRPI0412232-1A priority patent/BRPI0412232A/pt
Publication of WO2005002334A1 publication Critical patent/WO2005002334A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Definitions

  • the present invention relates to novel agrochemical formulations based on ethylene diamine alkoxylate derivative emulsifiers, a process for the preparation of these formulations, and their use for the application of the active compounds contained.
  • NMP N-methyl pyrrolidone
  • DMSO dimethyl sulfoxide
  • the concentrate is diluted with water.
  • a disadvantage of the known formulations is that during use, both the water-soluble solvent diffuses into the water and water is introduced into the emulsified oil droplet consisting of solvent and active ingredient. As a result, the suspension or the emulsion is destabilized and the active ingredient crystallizes out of the aqueous ready-to-use emulsion or suspension (spray mixture).
  • f) contain at least one compound which acts as an emulsion stabilizer and / or as a crystallization inhibitor.
  • the agrochemical formulations according to the invention can be prepared in which at least one agrochemical active ingredient, optionally mixed with a penetration promoter, optionally with an emulsifier, optionally with additives, ⁇ -butyrolactone and with a compound which acts as an emulsion stabilizer and / or as a crystallization inhibitor.
  • agrochemical formulations according to the invention are very suitable for the administration of the active compounds contained in plants and / or their habitat.
  • the formulations of the invention are characterized by a number of other advantages.
  • the formulations according to the invention when mixing the formulations according to the invention with water, only very little foaming occurs.
  • the formulations favor the biological effectiveness of the active components contained.
  • an increased storage stability is achieved in the formulations according to the invention, which otherwise can not be achieved due to the incompatibility of the active ingredients.
  • the invention preferably relates to agrochemical formulations which
  • the formulations according to the invention contain one or more agrochemical active substances.
  • Agrochemical active substances are to be understood as meaning all substances customary for plant treatment.
  • fungicides bactericides, insecticides, acaricides, nematicides, herbicides, plant growth regulators, plant nutrients and repellents.
  • fungicides include:
  • Imazalil imibenconazole, iminoctadine, Iprobenfos (IBP), iprodione, isoprothiolane,
  • Tebuconazole Tebuconazole, tecloftalam, techazene, tetraconazole, thiabendazole, thicyofen, thiophanate-methyl, thiram, tolclophos-methyl, tolylfluanid, triadimefon, triadimol, triazoxide, trichlamide, tricyclazole, tridemorph, triflumizole, triforin, triticonazole,
  • bactericides are:
  • insecticides examples include:
  • Bacillus thuringiensis 4-bromo-2- (4-chlorophenyl) -1- (ethoxymethyl) -5- (trifluoromethyl) -1H-pyrrole-3-carbonitrile, Bendiocarb, Benfuracarb, Bensultap, Betacyfluthrin, Bifenthrin, BPMC, Brofenprox, Bromophos A, Bufencarb, Buprofezin, Butocarboxin, Butylpyridaben,
  • Fenamiphos fenazaquin, fenbutatmoxide, fenitrothion, fenobucarb, fenothiocarb, fenoxycarb, fenpropathrin, fenpyrad, fenpyroximate, fenthione, fenvalerate, fipronil, fluazinam, fluazuron, flucycloxuron, flucythrinate, flufenoxuron, flufenprox, fluvalinate, fonophos, formothion, fosthiazate, fubfenprox, furathiocarb,
  • Imidacloprid Iprobenfos, isazophos, isofenphos, isoprocarb, isoxathione, ivermectin, lambda-cyhalothrin, lufenuron,
  • Parathion A Paxathion M, Permethrin, Phenthoate, Phorat, Phosalone, Phosmet, Phosphamidone, Phoxim, Pirimicarb, Pirimiphos M, Pirimiphos A, Profenophos, Promecarb, Propaphos, Propoxur, Prothiophos, Prothoate, Pymetrozine, Pyrachlophos, Pyridaphenthione, Pyresmethrin, Pyrethrum, Pyridaben, pyrimidifen, pyriproxifen,
  • Tebufenozide Tebufenpyrad
  • Tebupirimiphos Teflubenzuron
  • Tefluthrin Temephos
  • Terbam Terbufos
  • Tetrachlorvinphos Thiafenox, Thiamethoxam, Thiodicarb, Thiofanox, Thiomethone, Thionazine, Thuringiensin, Tralomethrin, Transfluthrin, Triarathen, Triazophos, Triazuron, Trichlorfon, Triflumuron, Trimethacarb,
  • herbicides examples include:
  • Anilides such as diflufenican and propa il; Arylcarboxylic acids, such as dichloro-picolinic acid, dicamba and picloram; Aryloxyalkanoic acids such as 2,4-D, 2,4-DB, 2,4-DP, fluroxypyr, MCPA, MCPP and triclopyr; Atyloxy-phenoxy-alkanoic acid esters, such as, for example, diclofop-methyl, fenoxaprop- ethyl, fluazifop-butyl, haloxy-pent-methyl and quizalofop-ethyl; Azinones, such as chloridazon and norflurazon; Carbamates such as chlorpropham, desmedipham, phenmedipham and propam; Chloroacetanilides such as alachlor, acetochlor, butachlor, metazachlor, metolachlor, pretilachlor and propachlor; Dinitroanilines such as oryz
  • chlorocholine chloride and ethephon examples of plant growth regulators chlorocholine chloride and ethephon may be mentioned.
  • plant nutrients include common inorganic or organic fertilizers for the supply of plants with macro and / or micronutrients.
  • repellents examples include diethyltolylamide, ethylhexanediol and butopyronoxyl.
  • fungicides are the strobilurin fungicides, e.g.
  • fungicides include prothioconazole, fluoxastrobin and trifloxystrobin.
  • prothioconazole and fluoxastrobin are particularly preferred.
  • formulations according to the invention optionally contain penetration enhancers.
  • Suitable penetration promoters in the present context are all those substances which are usually used to improve the penetration of agrochemical active substances into plants.
  • Alkanol alkoxylates of the formula are preferred.
  • R is straight-chain or branched alkyl having 4 to 20 carbon atoms
  • AO stands for an ethylene oxide radical, a propylene oxide radical, a butylene oxide radical or mixtures of ethylene oxide and propylene oxide radicals and
  • n stands for numbers from 2 to 30.
  • a particularly preferred group of penetration promoters are alkanol alkoxylates of the formula R-0 - (- EO-) n -H (Ia) in which
  • EO stands for -CH 2 -CH 2 -0-
  • ⁇ n stands for numbers from 2 to 20.
  • Another particularly preferred group of penetration promoters are alkanol alkoxylates of the formula
  • EO stands for -CH 2 -CH 2 -0-
  • PO is CH-CH-O-CH 3 p is from 1 to 10 and q is from 1 to 10.
  • Another particularly preferred group of penetration promoters are alkanol alkoxylates of the formula
  • EO stands for -CH 2 -CH 2 -0-
  • s stands for numbers from 1 to 10.
  • Another particularly preferred group of Penetrations wornem are alkanol alkoxylates of the formula
  • u stands for numbers from 6 to 17.
  • R is preferably butyl, isobutyl, n-pentyl, i-pentyl, neopentyl, n-hexyl, i-hexyl, n-octyl, i-octyl, 2-ethylhexyl, nonyl, i-nonyl, decyl, n Dodecyl, i-dodecyl, lauryl, myristyl, i-tridecyl, trimethyl-nonyl, palmityl, stearyl or eicosyl.
  • alkanol alkoxylate of the formula (Ic) is 2-ethyl-hexyl alkoxylate of the formula
  • EO stands for -CH 2 -CH 2 -0-
  • PO is CH-CH-0 and CH 3
  • the numbers represent 8 and 6 averages.
  • alkanol alkoxylates of the formula (Id) are compounds of this formula in which t stands for numbers from 9 to 12 and
  • u stands for numbers from 7 to 9.
  • alkanol alkoxylates are generally defined by the above formulas. These substances are mixtures of substances of the specified type with different chain lengths. For the indices, therefore, average values are calculated, which can also differ from whole numbers.
  • u • stands for the average value 8.4.
  • alkanol alkoxylates of the formulas given are known or can be prepared by known methods (cf., WO 98-35553, WO 00-35278 and EP-A 0 681 865).
  • Suitable additives which may be present in the formulations according to the invention are all customary formulation auxiliaries, such as e.g. organic solvents, defoamers, dispersants, preservatives, citric acid and its hydrates, dyes, fillers and even water.
  • customary formulation auxiliaries such as e.g. organic solvents, defoamers, dispersants, preservatives, citric acid and its hydrates, dyes, fillers and even water.
  • Suitable defoamers are conventional defoamers present in formulations of agrochemical active compounds. Examples include silicone oils, dispersions of silicone oils, magnesium stearate, phosphinic and Phosphbnklaren. Particularly preferred is Fluowet PL 80®.
  • Suitable organic solvents are all customary organic solvents which readily dissolve the agrochemical active ingredients used. Preference is given to aliphatic and aromatic, optionally halogenated hydrocarbons, such as toluene, xylene, Solvesso®, mineral oils, such as white spirit, petroleum, alkylbenzenes and spindle oil, tetrachloromethane, chloroform, methylene chloride and dichloromethane, as well as esters, such as ethyl acetate, fe lactones as well as lactolefins, such as N-methylpyrrolidone, N-octylpyrrolidone and N-methylcaprolactam, and also alkanecarboxamides, such as decanecarboxylic acid dimethylamide and octanecarboxylic acid dimethylamide, and also dimethylformamide.
  • aliphatic and aromatic, optionally halogenated hydrocarbons such as toluene, xy
  • water-soluble solvents such as, for example, N-methylpyrrolidone and DMSO.
  • DMSO dimethylpyrrolidone
  • Suitable emulsifiers are customary surface-active substances present in formulations of agrochemical active compounds.
  • ethoxylated nonylphenols polyethylene glycol ethers of linear alcohols, reaction products of alkylphenols with ethylene oxide and / or propylene oxide, ethylene oxide / propylene oxide block copolymers, polyethylene glycols and polypropylene glycols, furthermore fatty acid esters, alkylsulfonates, alkyl sulfates, aryl sulfates, ethoxylated arylalkylphenols, such as, for example Tristyrylphenol ethoxylate having an average of 16 ethylene oxide units per molecule, further ethoxylated and propoxylated arylalkylphenols and sulfated or phosphated arylalkylphenol ethoxylates or ethoxy and propoxylates. Particularly preferred are tristrylphenol alkoxylates. Very particular preference is given to tristyrylphenol ethoxylates together with tristyrylphenol
  • Suitable dispersants are all substances customarily used in crop protection agents for this purpose.
  • natural and synthetic, water-soluble polymers such as gelatin, starch and cellulose derivatives, in particular cellulose esters and cellulose ethers, fe polyvinyl alcohol, polyvinylpyrrolidone, polyacrylic acid, polymethacrylic acid and co-polymers of (meth) acrylic acid and (Meth) acrylic acid esters, and also neutralized with alkali metal hydroxide co-polymers of
  • Suitable preservatives are all substances usually present in plant treatment compositions for this purpose. Examples include Preventol® and Proxel®.
  • Suitable dyes are all customary for the production of pesticides inorganic or organic dyes. Examples include titanium dioxide, carbon black, zinc oxide and blue pigments.
  • Suitable fillers are all substances normally used for this purpose in crop protection agents. Preference is given to inorganic particles, such as carbonates, silicates and oxides having an average particle size of 0.005 to 5 .mu.m, more preferably from 0.02 to 2 microns. Examples include silicon dioxide, so-called highly disperse silica, silica gels, and natural and synthetic silicates and aluminosilicates.
  • Suitable compounds which act as emulsion stabilizers and / or crystallization inhibitors are all substances conventionally used for this purpose in crop protection agents.
  • Preferred are ethylene diamine alkoxylate derivatives. Particular preference is given to the ethylene diamine alkoxylate having the trade name Synperonic T / 304® from Uniqema.
  • the content of the individual components can be varied within a substantial range in the formulations according to the invention.
  • the concentrations of agrochemically active compounds are generally between 1 and 40% by weight, preferably between 20 and 30% by weight, of penetration promoters generally between 0 and 25% by weight, preferably between 10 and 25% by weight.
  • emulsifier generally between 5 and 30% by weight, preferably between 10 and 25% by weight, of additives in general between 0 and 40% by weight, preferably between 0 and 2% by weight, of compounds, the emulsion stabilizers and / or crystallization inhibitors generally act between 5 and 20 wt .-%, preferably between 5 and 15 wt .-%, of ⁇ -butyrolactone generally between 20 to 70 wt .-%, preferably between 30 and 50% by weight.
  • the preparation of the agrochemical formulations according to the invention takes place in such a way that the components are mixed together in the respectively desired ratios.
  • the agrochemical active substance is a solid substance, it is generally employed either in finely ground form or in the form of a solution or suspension in an organic solvent. If the agrochemical active ingredient is liquid, the use of an organic solvent is often unnecessary. It is also possible to use a solid agrochemical active ingredient in the form of a melt.
  • the temperatures can be varied within a certain range when carrying out the process according to the invention. It is generally carried out at temperatures between 0 ° C and 80 ° C, preferably between 10 ° C and 60 ° C.
  • the procedure is generally followed by mixing the penetration promoter with one or more active ingredients and optionally with additives, the emulsion stabilizer / crystallization inhibitor and ⁇ -butyrolactone.
  • the order in which the components are mixed together is arbitrary.
  • the procedure is to use the emulsion stabilizer / crystallization Synperonic T / 304® with one or more agrochemical active ingredients and other additives mixed and dispersing the resulting premix in water, so as to obtain emulsions, suspensions or solutions.
  • customary devices which are used for the preparation of agrochemical formulations are suitable.
  • agrochemical formulations according to the invention can be applied in the preparation forms customary for liquid preparations, either as such or after prior dilution with water, e.g. as emulsions, suspensions or solutions.
  • the application is carried out by conventional methods, e.g. by spraying, pouring or injecting.
  • the application rate of the agrochemical formulations according to the invention can be varied within a relatively wide range. It depends on the particular agrochemical active ingredients and their content in the formulations.
  • agrochemical active substances can be planted in a particularly advantageous manner and / or their habitat can be applied.
  • the application properties of the formulations can be tested in commercial field sprayers with different filter-nozzle combinations.
  • the formulations are diluted in the spray tank of the field sprayer with water, wherein the so-called spray mixture, in this case an emulsion forms.
  • spray mixture in this case an emulsion forms.
  • 1.5 1 of the emulsion concentrate are diluted with 200 1 of water.
  • the spray mixture is left standing for 24 hours and between the 9th and 10th application for 72 hours without stirring.
  • the filters and nozzles of the field sprayer are removed and checked for possible deposits and blockages.
  • Example 1 The formulation according to the invention of Example 1 showed after 12 applications (12 times 1.5 L formulation + 200 1 water) without intermediate cleaning of the spray tank a maximum filter occupancy with an 80 mesh nozzle filter of up to 10% and with a 50 esh nozzle filter of about 1%.
  • Comparative Example 3 showed a maximum filter coverage of up to 90% for an 80 mesh nozzle filler and about 25% for a 50 mesh nozzle filler.
  • Such filter pads of the nozzle filter already signify a significant impairment in the application of the spray mixture. With these filter pads in front of the spray nozzle, the spray fan drops (Angle with the spray mist exiting the spray nozzle) together and a complete blockage of the nozzle filter, so that no more product can escape from the spray nozzle, is imminent. By contrast, the formulation according to the invention of Example 1 shows no impairment.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

La présente invention concerne de nouvelles formulations agrochimiques à base d'émulsifiants dérivés d'éthylène-diaminalcoxylate, un procédé de fabrication de ces formulations et leur utilisation dans l'application des agents qu'elles contiennent.
PCT/EP2004/006673 2003-07-02 2004-06-21 Formulations agrochimiques WO2005002334A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
NZ544450A NZ544450A (en) 2003-07-02 2004-06-21 Agrochemical formulations comprising fluoxastrobin, prothioconazole or trifloxystrobin, gamma-butyrolactone and an ethylene diamine alkoxylate
EP04740113A EP1643833B1 (fr) 2003-07-02 2004-06-21 Formulations agrochimiques
CA002530883A CA2530883A1 (fr) 2003-07-02 2004-06-21 Formulations agrochimiques
PL04740113T PL1643833T3 (pl) 2003-07-02 2004-06-21 Formulacje agrochemiczne
DE502004008588T DE502004008588D1 (de) 2003-07-02 2004-06-21 Agrochemische formulierungen
US10/563,328 US7655599B2 (en) 2003-07-02 2004-06-21 Agrochemical formulations
BRPI0412232-1A BRPI0412232A (pt) 2003-07-02 2004-06-21 formulações agroquìmicas

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10329714.6 2003-07-02
DE10329714A DE10329714A1 (de) 2003-07-02 2003-07-02 Agrochemischen Formulierungen

Publications (1)

Publication Number Publication Date
WO2005002334A1 true WO2005002334A1 (fr) 2005-01-13

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ID=33521251

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2004/006673 WO2005002334A1 (fr) 2003-07-02 2004-06-21 Formulations agrochimiques

Country Status (9)

Country Link
US (1) US7655599B2 (fr)
EP (1) EP1643833B1 (fr)
AT (1) ATE415817T1 (fr)
BR (1) BRPI0412232A (fr)
CA (1) CA2530883A1 (fr)
DE (2) DE10329714A1 (fr)
NZ (1) NZ544450A (fr)
PL (1) PL1643833T3 (fr)
WO (1) WO2005002334A1 (fr)

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WO2006117192A2 (fr) * 2005-05-03 2006-11-09 Syngenta Participations Ag Compositions pesticides
WO2007017501A2 (fr) * 2005-08-11 2007-02-15 Basf Aktiengesellschaft Concentre emulsifiable
EP1695621A3 (fr) * 2005-02-26 2007-02-28 Bayer CropScience AG Formulation agrochimique contenant des agents phytosanitaires pour ameliorer leur activité et la tolerance des plantes
WO2008110274A2 (fr) * 2007-03-09 2008-09-18 Syngenta Participations Ag Associations de pesticides
WO2010043639A2 (fr) * 2008-10-16 2010-04-22 Basf Se Mélanges pesticides
WO2012000902A1 (fr) * 2010-06-29 2012-01-05 Bayer Cropscience Ag Compositions insecticides améliorées contenant une carbonylamidine cyclique
WO2014180850A1 (fr) * 2013-05-10 2014-11-13 Basf Se Concentrat émulsifiable comprenant un pesticide, un lactone, et un tri-c1-c6-alkyl phosphate
CN106857565A (zh) * 2017-03-07 2017-06-20 南京华洲药业有限公司 一种含氟嘧菌酯和丁香菌酯的杀菌组合物及其应用
EP3372079A1 (fr) 2017-03-06 2018-09-12 Bayer CropScience Aktiengesellschaft Nouveau concentré d'émulsion à base d'agents actifs agrochimiques
EP3415007A1 (fr) * 2017-06-12 2018-12-19 Bayer AG Formulations ptz à faible contenu de desthio

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DE10228103A1 (de) * 2002-06-24 2004-01-15 Bayer Cropscience Ag Fungizide Wirkstoffkombinationen
DE10335183A1 (de) * 2003-07-30 2005-02-24 Bayer Cropscience Ag Fungizide Wirkstoffkombinationen
DE10341945A1 (de) * 2003-09-11 2005-04-21 Bayer Cropscience Ag Verwendung von fungiziden Mitteln zur Beizung von Saatgut
DE10347090A1 (de) 2003-10-10 2005-05-04 Bayer Cropscience Ag Synergistische fungizide Wirkstoffkombinationen
DE102004049761A1 (de) * 2004-10-12 2006-04-13 Bayer Cropscience Ag Fungizide Wirkstoffkombinationen
DE102005023835A1 (de) * 2005-05-24 2006-12-07 Bayer Cropscience Ag Fungizide Wirkstoffkombination
KR101350756B1 (ko) * 2005-09-09 2014-02-17 바이엘 크롭사이언스 아게 살진균성 혼합물의 고형제제
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EP1643833A1 (fr) 2006-04-12
EP1643833B1 (fr) 2008-12-03
DE10329714A1 (de) 2005-01-20
CA2530883A1 (fr) 2005-01-13
US20060183639A1 (en) 2006-08-17
BRPI0412232A (pt) 2006-08-22
NZ544450A (en) 2009-07-31
US7655599B2 (en) 2010-02-02

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